ClinVar Miner

Submissions for variant NM_004588.5(SCN2B):c.67T>C (p.Leu23=)

dbSNP: rs2134623717
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002116231 SCV002442333 likely benign Atrial fibrillation, familial, 14 2021-09-17 criteria provided, single submitter clinical testing

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